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151.
Iva H?nová Radek Novotný Tomáš Vráblík Bohumír Lomský 《Environmental pollution (Barking, Essex : 1987)》2010,158(7):2393-2401
Malondialdehyde (MDA), a product of lipid peroxidation and biomarker of oxidative stress, is measured over the long term in spruce Picea abies needles under real conditions in three Czech mountain border areas. The trends presented collate the MDA content in spruce needles with ambient ozone, temperature and precipitation as casual, and defoliation as a subsequent factor for the period 1994-2006. We have found the overall decreasing trends in MDA and defoliation. The highest MDA and defoliation are recorded in the Jizerske, the lowest in the Krusne hory Mts. Out of the examined variables the MDA is predicted best by mean temperature in vegetation season, median of O3 concentrations and AOT40; these three variables account for 34% of MDA1 and 36% of MDA2 variability. Our hypothesis that higher ambient O3 exposure results in higher MDA contents in P. abies needles under real conditions has not been approved. 相似文献
152.
153.
Xueyuan Wang Xin-Zhong Liang Weimei Jiang Zhining Tao Julian X.L. Wang Hongnian Liu Zhiwei Han Shuyan Liu Yuyan Zhang Georg A. Grell Steven E. Peckham 《Atmospheric environment (Oxford, England : 1994)》2010,44(5):660-669
This study develops fine temporal (seasonal, day-of-week, diurnal) and vertical allocations of anthropogenic emissions for the TRACE-P inventory and evaluates their impacts on the East Asian air quality prediction using WRF-Chem simulations in July 2001 at 30-km grid spacing against available surface measurements from EANET and NEMCC. For NO2 and SO2, the diurnal and vertical redistributions of emissions play essential roles, while the day-of-week variation is less important. When all incorporated, WRF-Chem best simulates observations of surface NO2 and SO2 concentrations, while using the default emissions produces the worst result. The sensitivity is especially large over major cities and industrial areas, where surface NO2 and SO2 concentrations are reduced by respectively 3–7 and 6–12 ppbv when using the scaled emissions. The incorporation of all the three redistributions of emissions simulates surface O3 concentrations higher by 4–8 ppbv at night and 2–4 ppbv in daytime over broad areas of northern, eastern and central China. To this sensitivity, the diurnal redistribution contributes more than the other two. 相似文献
154.
155.
Naser?A.?Anjum Iqbal?AhmadEmail author Mónica?Válega Etelvina?Figueira Armando?C.?Duarte Eduarda?Pereira 《Environmental science and pollution research international》2013,20(6):3910-3922
Efficient and sustainable management of rapidly mounting environmental issues has been the focus of current intensive research. The present study aimed to investigate the impact of plant phenological development stage variation on mercury (Hg) tolerance, accumulation, and allocation in two salt marsh macrophytes Triglochin maritima and Scirpus maritimus prevalent in historically Hg-contaminated Ria de Aveiro coastal lagoon (Portugal). Both plant samples and the sediments vegetated by monospecific stands of T. maritima and S. maritimus were collected from reference (R) and sites with moderate (M) and high (H) Hg contamination in Laranjo bay within Ria de Aveiro lagoon. Hg tolerance, uptake, and allocation in T. maritima and S. maritimus, physico-chemical traits (pH, redox potential, and organic matter content) and Hg concentrations in sediments vegetated by these species were impacted differentially by phenological development stages variation irrespective of the Hg contamination level. In T. maritima, Hg concentration increased with increase in Hg contamination gradient where root displayed significantly higher Hg followed by rhizome and leaf maximally at H. However, in S. maritimus, the highest Hg concentration was perceptible in rhizome followed by root maximally at M. Between the two studied plant species, S. maritimus displayed higher Hg tolerance index (depicted by higher plant dry mass allocated to reproductive stage) and higher available Hg at M (during all growth stages) and H (during senescent stage) when compared to T. maritimus. Both plant species proved to be Hg excluder (low root/rhizome–leaf Hg translocation). Additionally, T. maritima also acted as Hg stabilizer while, S. maritimus as Hg accumulator. It can be inferred from the study that (a) the plant phenological development stage variations significantly influenced plant Hg sensitivity by impacting sediment chemistry, plant growth (in terms of plant dry mass), Hg accumulation, and its subsequent allocation capacity, contingent to Hg contamination gradient; (b) S. maritimus accumulated higher Hg but restricted its translocation to above-ground part using exclusion process at both M and H due to its accelerated growth during Hg-tolerant reproductive/metabolically active phenological development stage greater than its counterpart T. maritima; and (c) the studied salt marsh plants although hailed from the same C3 and monocot group did not necessarily display similar phenotypic plasticity and behavior towards Hg-contaminated scenario during their life cycle. 相似文献
156.
Alice Gitchell R. Simonaitis Julian Heicklen 《Journal of the Air & Waste Management Association (1995)》2013,63(4):357-361
In urban atmospheres hydrocarbons promote the conversion of NO to NO2 under the influence of sunlight, ultimately giving rise to photochemical smog. The conversion results from a long chain process with HO radicals as the chain carrier. If this chain could be interrupted by suitable radical traps, the formation of photochemical smog would be inhibited. In this paper we report the results of studies using phenol, benzaldehyde, and aniline as inhibitors. Mixtures containing 16 mTorr C3H6, 8 mTorr NO, ~85 Torr 02, and the addi tives were irradiated at 25°C. The NO2 pressure was monitored photometrically. In the absence of additive, the NO2 pressure first increases with irradiation time reaching a maximum conversion corresponding to 70% of the NO at 1 2 minutes. As the radiation time is lengthened, the NO2 pressure drops. With the additive present, the formation of NO2 is delayed. The time to reach the maximum percent conversion of NO to N02 becomes 20, 22, 31, and 40 minutes respectively, for 13 mTorr C6H5OH, 2 mTorr C6H5CHO, 8 mTorr C6H5CHO, and 4.1 mTorr C6H5NH2 added. The problems and possibilities of adding inhibitors to the atmosphere to control air pollution are discussed. 相似文献
157.
Alice Gitchell R. Simonaitis Julian Heicklen 《Journal of the Air & Waste Management Association (1995)》2013,63(8):772-775
Additional inhibitors for the conversion of NO to NO2 in C3H6—NO—02 irradiated mixtures have been tested at 25°C. These mixtures initially contained 16 mTorr C3H6, 8 mTorr NO, 0.012 mTorr NO2, additive, and enough O2 to bring the total pressure to 100 Torr. The NO2 pressure was monitored photometrically. In the absence of additive, the NO2 pressure first increases with irradiation time reaching a maximum conversion at about 15 minutes. As the irradiation time increases beyond 15 min, the NO2 pressure drops. Before adding the inhibitors, runs were done with 10 Torr of CO added, and in these runs the conversion was speeded so that the maximum in NO2 pressure occurred at 10 min. This enhancement in conversion rate is considered to be diagnostic for the presence of HO radicals. Next 10-min irradiations were done with various amounts of hexafluorobenzene (C6F6), nitrobenzene (C6H5NO2), or naphtha lene (C10H8) added. The NO2 pressure was reduced to one-half its value in the absence of inhibitor with 270 mTorr C6F6’, 220 mTorr C6H5N02, or 4 mTorr C10Hg. The C10H8 is a very efficient inhibitor, but additions of up to 1 8.5 mTorr C10H8 did not reduce the N02 pressure to zero. Studies of the percent conversion of NO to NO2 vs. irradiation time were done with either 4.2 mTorr C10H8 or 40 mTorr 2,6-di-ferf-butyl-4-methylphenol (Ph) added. In the former case the peak conversion was delayed from 15 to 22 min, while in the latter case no delay occurred. However, with the Ph added, there appeared to be some reduction in the maximum value of percent conversion. 相似文献
158.
Liu X Sun L Yuan D Yin L Chen J Liu Y Liu C Liang Y Lin F 《Environmental science and pollution research international》2011,18(8):1324-1332
Background and purpose
More and more coal-fired power plants equipped with seawater flue gas desulfurization systems have been built in coastal areas. They release large amount of mercury (Hg)-containing waste seawater into the adjacent seas. However, very limited impact studies have been carried out. Our research targeted the distribution of Hg in the seawater, sediment, biota, and atmosphere, and its environmental transportation. 相似文献159.
Vijgen J Abhilash PC Li YF Lal R Forter M Torres J Singh N Yunus M Tian C Schäffer A Weber R 《Environmental science and pollution research international》2011,18(2):152-162
Purpose
Hexachlorocyclohexane (HCH) isomers (??-, ??- and ??- (Lindane)) were recently included as new persistent organic pollutants (POPs) in the Stockholm Convention, and therefore, the legacy of HCH and Lindane production became a contemporary topic of global relevance. This article wants to briefly summarise the outcomes of the Stockholm Convention process and make an estimation of the amount of HCH waste generated and dumped in the former Lindane/HCH-producing countries.Results
In a preliminary assessment, the countries and the respective amount of HCH residues stored and deposited from Lindane production are estimated. Between 4 and 7 million tonnes of wastes of toxic, persistent and bioaccumulative residues (largely consisting of alpha- (approx. 80%) and beta-HCH) are estimated to have been produced and discarded around the globe during 60 years of Lindane production. For approximately 1.9 million tonnes, information is available regarding deposition. Countries are: Austria, Brazil, China, Czech Republic, France, Germany, Hungary, India, Italy, Japan, Macedonia, Nigeria, Poland, Romania, Slovakia, South Africa, Spain, Switzerland, Turkey, The Netherlands, UK, USA, and former USSR. The paper highlights the environmental relevance of deposited HCH wastes and the related POPs?? contaminated sites and provides suggestions for further steps to address the challenge of the legacy of HCH/Lindane production.Conclusion
It can be expected that most locations where HCH waste was discarded/stockpiled are not secured and that critical environmental impacts are resulting from leaching and volatilisation. As parties to the Stockholm Convention are legally required to take action to stop further POPs pollution, identification and evaluation of such sites are necessary. 相似文献160.
The World Bank used the Consumer Price Index (CPI) to calculate changes in the world poverty level (measured in U.S. dollars)
prior to 1982. In 1983, the U.S. Bureau of Labor Statistics (BLS) replaced the CPI with several indices including CPI-W which
was then adopted by the World Bank. This caused the inflated rate of the U.S. dollars and the percentage of the world population
in poverty to be dramatically underestimated. This new incorrect procedure gives 25% (1.5 million) below the poverty line
in 2005, while the more appropriate procedure (described herein) gives 52% (3.3 million in 2005). The rapid rise of the poverty
line (using the preferable CPI) starting in 1987 occurred at nearly the same time as the peak in per capita annual cereal
production. 相似文献